Overtube introducer for use in endoscopic bariatric surgery

ABSTRACT

This application describes an overtube device that gives diagnostic and/or therapeutic access to body cavities using natural orifices of the body. The overtube includes an elongate flexible body having a distal portion deflectable in response to activation of a control cable. Proximal features of the overtube include an insufflations port and seals for minimizing loss of insufflations pressure around the shafts of instruments passed through the tube. In some embodiments, retractor elements are including on the distal portion of the overtube.

PRIORITY

This is application claims priority to U.S. Provisional Application No.60/950,584, filed Jul. 18, 2007

BACKGROUND OF THE INVENTION

This application describes an overtube/introducer device that givesaccess to body cavities using natural orifices of the body (e.g.,esophagus, anus, vagina) for a variety of therapeutic and/or diagnosticprocedures. In a particular application, the overtube/introducer enablesthe introduction of devices into the gastrointestinal tract of a patientvia the mouth and esophagus. Therapies to be carried out using theintroducer can include procedures designed for the treatment of obesity.The disclosed overtube provides in and out access to the targetedprocedural site and protects the body tissue during the procedure fromtrauma.

The disclosed overtube is suitable for use in an exemplary procedure inwhich the geometry of the stomach is modified and implantable devicesare deployed. The procedure is preferably performed entirely through thenaturally existing orifice of the mouth, without additional externalincisions.

The exemplary procedure is initiated with the introduction of anovertube into the mouth and, at a minimum, past the pharynx of a patientbut preferably reaching and sealing against the lower esophagealsphincter (LES). For reference, FIG. 1 shows the anatomy of the humanhead and stomach, with reference numerals identifying the followingfeatures:

-   -   1. Body of stomach    -   2. Fundus    -   3. Anterior wall    -   4. Greater curvature    -   5. Lesser curvature    -   6. Lower esophageal sphincter (LES)/gastroesophageal junction    -   9. Pyloric sphincter    -   10. Pyloric antrum    -   11. Pyloric canal    -   12. Angular notch    -   13. Gastric Canal    -   14. Rugal folds

The entire exemplary procedure is preferably performed under directendoscopic visualization, obtained by inserting a flexible endoscopeinto the overtube prior to its introduction into the patient, though theprocedure (or individual steps of the procedure) may also be performedwithout direct visualization. In cases where an endoscope is used, theendoscope's distal tip may be inserted into a flexible Bougie thatincorporates a central lumen allowing direct line-of-sight for theendoscope's illumination and visualization optics. The endoscope withthe installed Bougie may then be inserted into the overtube's centrallumen until the Bougie protrudes just past the overtube's distal end.This provides a gentle leading edge that facilitates insertion of theBougie, overtube and endoscope into the patient's esophagus.

Alternatively the overtube may be inserted over a guide wire; theguidewire inserted under direct visualization using a standardendoscope. A transition member is positioned between the inside diameterof the overtube and the outside diameter of the guidewire providing fora smooth transition. This transition is preferably a long taper, andcomposed of a soft, flexible material such as silicone.

Once the overtube, endoscope and Bougie have reached the desiredposition within the esophagus, the endoscope and Bougie are withdrawnfrom the overtube, and the overtube is left in position. The overtube isnow in a position to facilitate the introduction of other tools anddevices needed to perform subsequent steps.

With the overtube in the desired position, a special-purpose stapler isinserted which will be used to prepare sites within the stomach walltissue that will serve as mounting points for implantable devices to beinstalled in later steps. Staplers suitable for this procedure includethose disclosed in the following U.S. Applications:

-   -   U.S. application Ser. No. 11/542,457, filed Oct. 3, 2006,        Attorney Docket BARO-1110;    -   U.S. application Ser. No. 11/900,757, filed Sep. 13, 2007,        Attorney Docket BARO-1310.    -   U.S. application Ser. No. 12/119,329, filed May 12, 2008,        Attorney Docket BARO-1610.    -   U.S. application Ser. No. 12/050,169, filed Mar. 18, 2008,        Attorney Docket BARO-1900.

In one such stapler, the leading distal tip of the stapler mechanism iscovered with a compliant, bullet-shaped, Bougie end cap, andincorporates a side-looking window. The smooth Bougie shape of the endcap facilitates introduction of the stapler into the overtube and pastthe distal end of the overtube into the patient's esophagus or stomach.The side window allows stomach wall tissue to be drawn between thestapler jaws prior to the application of staples. The staplerincorporates a passive flexible length which allows the device to bendfreely between the user controls at the proximal end and the staplermechanism at the distal end. Insertion of the stapler is preferablyperformed under direct endoscopic visualization, with an endoscopepositioned next to the stapler such that its camera optics are locatedslightly proximal of the stapler's distal end. In this way, the positionof the stapler may be visualized at all times, relative to its positionwithin the overtube, esophagus and stomach. However, insertion of thestapler may optionally be performed without using an endoscope forvisualization.

With the stapler inserted into the stomach, it may then be positionedrelative to the stomach wall near the lower esophageal sphincter asdesired. In order to achieve the desired position and visualization, itmay be necessary to withdraw or further insert the overtube, or tomanipulate certain features of the overtube, in such a way that itadvantageously alters the geometry of the tissue and/or the overtube'srelative position. When the position of the stapler is judged to becorrect, suction is applied to draw stomach wall tissue into the staplerend cap's side-looking window. This positions the stomach wall tissuebetween the jaws of the stapler, which are then approximated via aphysician-controlled actuator to clamp the tissue firmly in position.Once the tissue has been securely fixtured, the suction may be released,as it is no longer needed to retain the stomach tissue. Staples are thendeployed by means of a second physician-controlled actuator through theplication, or fold, of stomach tissue between the stapler's jaws tocreate circular rings about a central point. A hole is created in theplication of stomach tissue at the center of the pattern of stapessimultaneous to the application of the staples. The hole and surroundingcircular array of staples create a secure and durable mounting point(e.g., for implantable devices), and will be used in later steps of theprocedure. Once the staples have been deployed and the mounting pointhas been created, the physician releases the plication from thestapler's jaws and any remaining suction. The stapler and endoscope arethen withdrawn from the overtube.

For staplers that must be re-loaded prior to the creation of the nextmounting point, the stapler is withdrawn from the overtube and thedistal stapling mechanism is then reloaded. For self-reloading staplermechanisms, this step is not required. If reloading is required and hasbeen performed, the reloaded device, Bougie end cap and endoscope arereinserted into the overtube. The process of positioning the staplermechanism within the stomach described above is repeated so that thenext mounting point is identified and created. This process is repeatedto produce one or more anchor points, but preferably four mountingpoints are created. These mounting points may be anywhere within thestomach, but they are preferably located at the 3, 6, 9 and 12 o'clockpositions, a fixed distance away from the lower esophageal sphincter. Ifthe mounting points are to be used as anchor points for a flowrestrictor of the type used to restrict/obstruct passage of food fromthe esophagus into the stomach, the preferential distance of themounting points is such that the position of the exit of a restrictorattached at the mounting points will be immediately adjacent the loweresophageal sphincter. Exemplary restrictor devices include but are notlimited to those disclosed in U.S. Pat. Nos. 6,675,809, 6,845,776,7,097,665, and 7,146,984, U.S. application Ser. No. 10/345,666, filedJan. 16, 2003, Attorney Docket No. BARO-300, and U.S. application Ser.No. ______, Endoscopic Implant System and Method, Attorney DocketBARO-2010, filed Jul. 17, 2008.

Once the desired mounting points have been created with the stapler, thestapler is withdrawn. Next, highly compliant anchors are installedthrough the hole at the center of each of the mounting points. Theanchors have a rivet-like shape with large retaining heads on eitherend. The anchors are intended to be installed in the holes at the centerof the mounting points, remain in position indefinitely or untilremoved, and be easily removable. The anchors are configured such thatthey may be grasped and pulled from one end (herein referred to as the“leading end”), and the resulting tension causes the leading endretaining head to change profile so that it may be drawn through thehole in a mounting point. The other end of the anchor (herein referredto as the “following end”) is designed so that tension resulting fromdrawing it through the mounting hole does not result in a change to itsprofile, so it cannot be drawn through the mounting hole. Anchors ofthis type are described in U.S. application Ser. No. ______, EndoscopicImplant System and Method, Attorney Docket BARO-2010, filed Jul. 17,2008

Anchors are positioned in each of the mounting holes by means ofgraspers or similar instruments, which pull them, leading end first,through the mounting holes. Once the anchors are installed, theinstruments required to insert them are withdrawn from the overtube.

Finally, a restrictor is inserted into the stomach via the overtube. Therestrictor is attached to the anchors, and will remain in the stomachafter the procedure for an indefinite period of time, such as the pointin time when a physician determines the patient has achieved sufficientweight loss. The restrictor is attached to the anchors by drawing theleading end of the anchors through mounting holes in the restrictorusing graspers or other instruments, as appropriate.

When the restrictor is attached to the anchors, the procedure iscomplete and the overtube may be withdrawn from the patient, along withany tools remaining in the lumen it defines (e.g., endoscope, graspers,etc.).

Upon completion of the procedure, the overtube has enabled thedeployment of a restrictor, which is attached to anchors that have beenimplanted into stapled plications in the stomach wall. The passage offood into the stomach from the esophagus has been restricted, alteringthe patient's feelings of satiety and eating habits.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 schematically illustrates certain aspects of the anatomy of thehead and stomach;

FIG. 2 is a side elevation view of an embodiment of an overtube

FIG. 3 is a side elevation view of a distal portion of the overtube ofFIG. 2.

FIG. 4A is a side elevation view of an alternate portion of an overtube,showing expansion of the distal portion in response to introduction ofan instrument into the overtube.

FIG. 4B illustrates a reinforcing ring suitable for use in thedeformable overtube of FIG. 4A and shows degrees of deformation of thereinforcement ring in response to instrument advancement through theovertube.

FIG. 4C is a cross-section view of the tube of FIG. 4A, shown astransparent to permit viewing of an alternate reinforcement. The figureshows deformation of the reinforcement ring in response to instrumentadvancement through the overtube. FIG. 4D is similar to FIG. 4C andshows yet another alternate reinforcement.

FIG. 5A-5C are a sequence of steps illustrating one embodiment of anovertube manufacturing technique

FIG. 6A shows three cross-section views of arrangements of alternatingthermoplastic elements with and without wire cores that may be used toform a wall of an overtube in the method of FIGS. 5A-5C.

FIG. 6B is a longitudinal cross-section view of one embodiment of anovertube made using thermoplastic and wire core arrangements of the typeshown in FIG. 6A.

FIGS. 6C and 6D is similar to the drawings of FIG. 6A but shows analternate arrangement of thermoplastic elements and wire core elements.

FIG. 7 illustrates an alternate method of making an overtube using athin sheet of thermopolymer or other suitable material.

FIGS. 7A-7B are cross-section views illustrating various lumenarrangements for the overtube.

FIG. 8 is a side elevation view of a distal portion of an overtubehaving a bougie positioned at its distal end.

FIG. 8A is a side elevation view of a distal portion of an overtubehaving a transition member and endoscope extending from its distal end.

FIG. 8B is a side elevation view of a distal portion of an overtubehaving a transition member and a guidewire endoscope extending from itsdistal end.

FIG. 9A is a side elevation view of a distal portion of an overtubehaving an umbrella-shaped leading element.

FIG. 9B is similar to FIG. 9A and illustrates inversion of the umbrellaelement for withdrawal.

FIG. 9C is similar to FIG. 9A and illustrates advancement and collapseof the umbrella element for withdrawal.

FIG. 10 is a side elevation view of a distal portion of an overtubehaving spreadable finger elements.

FIG. 11A is a side elevation view of a distal portion of a secondembodiment of an overtube having spreadable finger elements, showing thefinger elements in the retracted position.

FIG. 11B is similar to FIG. 11A and shows the finger elements in theexpanded position.

FIG. 12A shows an alternative arrangement of finger elements which maybe positioned on the distal end of an overtube as in FIG. 10.

FIG. 12B shows the finger elements of FIG. 12A in a partially expandedposition.

FIG. 12C shows the finger elements of FIG. 12A in the fully expandedposition.

FIGS. 13A and 13B are perspective views of the distal portion of anovertube showing alternative shapes finger elements at the distal end ofan overtube.

FIG. 13C is a perspective view of a vacuum cup positioned on a fingerelement.

FIG. 13D is a perspective view of a distal portion of an overtubeshowing an implant device mounted to the finger elements.

FIG. 14 is a perspective view illustrating a control mechanism for usewith expandable members such as the finger elements of FIGS. 10-13D.

FIG. 15 is a perspective view illustrating a distal portion of anovertube having an alternate arrangement of expandable elements in theform of a pair of expandable hoops.

FIG. 16 is a side elevation view of an embodiment of an overtube havingan articulating distal portion.

FIG. 17A illustrates an embodiment of a spring assembly suitable for usein the overtube of FIG. 16.

FIG. 17B shows the spring assembly of FIG. 17A in an articulatingposition.

FIG. 18A is a side view of a distal portion of an overtube utilizing astacked ring construction for the articulating section.

FIG. 18B is similar to FIG. 18A and shows the articulating section in anarticulated position.

FIGS. 18C and 18D are similar to FIGS. 18A and 18B and show an alternateconfiguration of stacked ring elements.

FIG. 19 is a perspective view showing an alternate arrangement of ringelements suitable for use in the articulating section.

FIG. 20 is a side elevation view of a distal portion of an overtubeillustrating optional inner and outer sheaths covering the articulatingsection.

FIG. 21 is a cross-sectional side view of an overtube with an instrumentpositioned in the lumen of the overtube, and illustrates the use ofmagnetic indexing.

FIG. 22 is a cross-sectional side elevation view showing a distalportion and intermediate portion of an overtube together with proximalcontrol features for use in controlling the articulating section of theovertube.

FIG. 23 illustrates articulating control features utilizing separatespools for each pullwire cable.

FIG. 24A is a perspective view of a portion of a spool and knob having aselection of cable attachment points allowing for selection and/oradjustment of cable length.

FIG. 24B is a side elevation view showing a barrel adjuster suitable forfine tuning cable length.

FIG. 25 shows perspective view and proximal end views of an overtubehaving depth and angle markings.

FIG. 26 shows a distal end view, side elevation view, and proximal endview of an overtube and illustrates color coding of angle markings.

FIG. 27 is a side view of a distal portion of an overtube, illustratingthe use of color coded markers positioned within the field of view of anendoscope used in combination with the overtube.

FIG. 28 is a perspective view of a proximal end of an overtube andillustrates a terminating end ring.

FIG. 29 is a plan view of a proximal end of an overtube and illustratesan iron intern ring.

FIG. 30 is a perspective view of a proximal portion of an overtubeshowing the use of steering controls and expandable element controls oniron an intern ring of the type shown in FIG. 29.

DETAILED DESCRIPTION

The present invention comprises an overtube intended to be insertedtrough the mouth into the esophagus of a patient, and extend at leastpast the pharynx, but preferably far enough for the distal end to sealagainst the lower esophageal sphincter (LES) at the junction between thestomach and the esophagus. The overtube incorporates features thatenable it to facilitate the procedure described in the Backgroundsection above though is not restricted to that single procedure. Theprimary purpose of the present invention is to create and maintain apatent lumen that provides access from the mouth of a patient to thestomach. The outer diameter of the overtube's insertable length allowsit to fit within, and be insertable into, a patient's gastrointestinaltract from the mouth to the stomach. The outer surface of the insertablelength of the overtube is sufficiently lubricious to allow for itsintroduction into the esophagus and subsequent manipulations (e.g.,further insertion or withdrawal, rotation), and/or is compatible withlubricants commonly used for such procedures. The inner diameter of theovertube's insertable length is sufficiently large to accommodate theinsertion of the instruments described in the Background section (e.g.,stapler, endoscope, graspers, etc.). Alternatively, the Overtube may becomposed of multiple lumens allowing multiple tools to be insertedwithout interfering with each other. The inner surfaces of theovertube's insertable length are sufficiently lubricious to allow theinsertion of instruments and devices, and/or are compatible withlubricants commonly used for such purposes. The overtube conforms to thepatient's anatomy and protects anatomical features (e.g., the pharynx,esophagus, lower esophageal sphincter, etc.) from injury that may resultfrom the insertion and manipulation of instruments during the procedure.Further, the overtube provides a means to control the position relativeto the LES along the axis of insertion. The position of the distal endof the overtube may be controlled by means of insertion and withdrawalof the instrument (the “Z-level”), by means of rotation of (torquing)the insertable length of the overtube, and by optionally incorporatingan articulatable, steerable, lockable section somewhere within theinsertable length. The overtube assembly may also incorporate expandableelements at or near the distal tip that assist in creating a volumewithin the stomach, reshaping the walls to facilitate visualization andaccess. The overtube possesses sufficient tensile, compressive and hoopstrength to resist excessive deformation (e.g., extension, compression,collapse, kinking) during use. Materials suitable for short-term mucosaltissue contact are preferable for use in the overtube, e.g., stainlesssteel, nitinol, silicone, urethanes, PEEK, PVC, etc.

Overview and System Layout

FIG. 2 shows a general system diagram of the overtube 100, and indicatesthe configuration and names of system components. The insertable lengthof the overtube 101 is comprised of at least one passive section 102 andoptionally at least one articulatable, lockable section 103, which maybe steered by means of controls 104 at the proximal end 105 of theassembly. The proximal end also incorporates a terminating end piece 106and an iron intern ring 107, which serve to support and orient thedevice during use. At the distal end 108 of the overtube, spreadablefingers 108 may be incorporated to facilitate maneuvers during aprocedure. The configuration of the spreadable fingers is determined bycontrols 104 at the proximal and 105. The construction of the overtubemay include some or all of these elements, in different combinations, orit may omit elements, depending on the configuration. This disclosure isintended to include all combinations of inclusion or exclusion of theseelements.

Insertion Tube Characteristics

One embodiment of the present invention's insertable length 101 (FIG. 3)consists of a compliant, flexible, hollow tube. The preferred dimensionsof the tube are approximately 38-42 cm (15-16.5 in.) in length (L), withouter diameter (OD) of approximately 1.0-2.0 cm (0.780 in.) (preferably2.0 cm, but up to approximately 2.2 cm), inner diameter (ID)approximately 1.8 cm (0.700 in.) and wall thickness (T) approximately0.1-0.2 cm. Larger diameters are preferable when the anatomy willaccommodate it, however tubes having smaller dimensions (including thosehaving a diameter proportioned to only accommodate small instruments orendoscopes) are also considered within the scope of this invention. Thetube is supported internally at least part of its length by a springformwire 112, intended to support the compliant material comprising the tube110, and to improve the tube's patency when bent, and to improve thetube's torsional rigidity to facilitate rotating the overtube when insitu during a procedure (its “torquability”). The springform wirereinforcement may extend the full length of the tube, or it mayoptionally terminate some distance short of the distal or proximal tip.The reinforcement 112 may be encapsulated within the overtube's wall ina thermopolymer or thermoset polymer matrix. The overtube is designed tobe compliant and flexible, enabling it to follow the contours andnavigate around features of the patient's anatomy, and is capable ofconforming to curves with a radius of curvature of at least 1.5 in.

The tube 110 may also incorporate a thin woven mesh, encapsulated withinthe compliant material as described above, either in conjunction withthe springform wire 112 or in lieu of such a wire. The woven mesh may bemade of stainless steel, for instance, or aluminum, or any of a varietyof polymeric materials. The purpose of embedding mesh within the tube isto substantially increase its torquability while having a minimal effecton its resistance to bending or its minimum radius of curvature.

The outer surface of the insertable length of the overtube should besufficiently lubricious to allow for its introduction into the esophagusand subsequent manipulations (further insertion or withdrawal,rotation), and/or be compatible with lubricants commonly used in suchprocedures. The inner surfaces of the overtube's insertable lengthshould also be sufficiently lubricious to accommodate the insertion ofinstruments and devices, and/or be compatible with lubricants typicallyused in such applications. In order to achieve sufficient lubricity,inherently lubricious materials may be selected (e.g., PTFE), orcoatings may be applied to base materials (e.g., hydrophilic orhydrophobic coatings). Features that prevent locking or binding betweencomponents may also be incorporated, such as serrations or surfacefeatures similar to those seen on knives designed for slicing meat. Suchfeatures facilitate sliding, rather than binding, when elements aremoved relative to one another.

The tube 110 may include a single or large central lumen 114 a as shownin FIGS. 7A and 7B, or multiple smaller lumens 114 b as in FIG. 7C.Additionally, the tube may incorporate numerous channels 114 ccompletely or partially within the wall. (FIG. 7B). In this way, itcomprises a multi-lumen tube, with at least one large central lumenwhose primary purpose is facilitating the introduction of instrumentsand devices to the stomach, and at least one much smaller lumen, throughwhich control cables, fluids, etc. may be routed between the proximaland distal end of the device, or to intermediate points between theends. In this way, the device presents a single, smooth outer surface tothe patient, rather than having any ancillary elements separate from theovertube's insertable section itself in contact with a patient'sgastrointestinal tract tissue. This provides protection for thecomponents that may be routed within these lumens, and increases controlof cleanliness and thus device function, as well as reduction ofrequirements for biocompatibility. In some cases, the small channels orlumens 114 c within the wall of the overtube may serve more than onepurpose: for example, the compressive housing of a Bowden cable may beunnecessary when the control cable is routed within one of the smalllumens in the overtube itself, eliminating a component and simplifyingthe design. For reference, a Bowden cable is comprised of an innercontrol cable which is housed in an outer housing designed to withstandcompressive loads, often a coil tube. Displacements at the proximal endof the inner cable relative to the coil tube housing of a Bowden cableare transmitted to the distal end of the inner cable, and can be used asan actuator to create useful forces and motion relative to the cablehousing.

The construction of the overtube may also be such that it may beexpanded as necessary after it has been placed within a patient'sanatomy. In the event that large instruments or devices are to beinserted through the overtube into the stomach, it may be beneficial toallow the overtube to expand to accommodate such large components thatmay otherwise fit too tightly or not at all, and to then return to itsunexpanded diameter following passage of the large device. This isillustrated in FIG. 4A. One means of accomplishing this is to form thereinforcing wire rings 112 a or coil used to support the overtubestructure into elliptical shapes, rather than a circular profile. Suchrings could also be encapsulated within a thermopolymer or thermosetpolymer matrix, as described above. If the elliptical reinforcing ringsare tilted in aspect ratio, as shown in FIG. 4B, the cross sectionalshape of the overtube's insertable length is circular under normalcircumstances. However, when a large instrument is inserted into theovertube's central lumen to the stomach, the elliptical reinforcingrings comprising the overtube's structural supports can change aspect topresent a larger cross sectional area, thus allowing the largeinstrument to pass through. FIG. 4C shows another embodiment, whichrelies upon support rings 112 b which are not continuous closed forms,but rather are partial rings which have a shape resembling the letter“C”. The shape of the partially ring can optionally be in a closeddefault configuration to resemble the letter “O”, with the ends of thering touching or overlapping, which then dilate and open a gap whenexpansion forces are applied. Alternatively, more than one wire shape112 c can be combined to create a structure which spans the fullcircumference of the tube (FIG. 4D). In cases where the ends of the wireendpoints overlap, a fold 116 may be introduced in the thermopolymer orthermoset polymer matrix encapsulating the support to facilitate suchdilation (FIG. 4D).

One means of manufacturing the insertable length of the overtubeassembly as described (with reinforcing elements encapsulated within amatrix) is to start with a wire 112 which is coated with a thermopolymer113. This wire may be coiled around a mandrel 118 having the desiredouter diameter or profile (the mandrel's outer diameter need not beconsistent). This is depicted in FIG. 5A Heat shrink 120 may then beplaced over the entire wound wire and mandrel 118 and heat applied, forexample with a heat gun 122 or hot box, causing the heat shrink to relaxover the wire (FIG. 5B). With the appropriate amount of heat addition,the heat shrink material and any coatings on the wire core will thenflow around and encapsulate the wire 112 (FIG. 5C). Once the wire andthermopolymer assembly is complete, the supporting mandrel 118 may beremoved, leaving a flexible, hollow tube. The same technique can beperformed with a wire mesh in addition to the coil of wire, or insteadof the coil of wire. The pitch of the wire wound around the mandrel 118may also be varied prior to the application of heat shrink. This may beaccomplished by alternating thermoplastic elements that have no wirecore between windings 113 of those that have the wire core 112, as shownin FIG. 6A. After the application of heat and the flow of thethermopolymer, this results in differences in the space between eachturn of wire, affecting the overall pitch (FIG. 6B). The profile of thethermopolymer elements that have no wire core may be round, square,rectangular, or any other desired shape, and the wire 112 need not beoriginally coated with thermoplastic, nor are they necessarily the samesize (FIG. 6C). The cross sectional area of the thermopolymer-onlyelements need not have the same cross-sectional area as those containingwire (FIG. 6D).

Another means of manufacturing the insertable length of the overtube isto wrap at least one layer of a thin rolled sheet 120 a around a mandrel118, and then fuse the layers together using heat, adhesives or chemicalmeans. This is shown in FIG. 7. Reinforcing elements, e.g., wire and/ormesh, may be incorporated underneath, in between or on top of the rolledsheets in order to create an overtube with encapsulated supportelements.

Bougie at Distal End

The distal tip may maintain the same outer diameter (herinafter “OD”),inner diameter (hereinafter “ID”) and wall thickness as the rest of thetube, or it may taper slightly to form a gentle curve. When an optionaltaper is incorporated into the distal tip, this serves to facilitateintroduction into a patient's gastrointestinal tract, as well as helpingto prevent tissue from being drawn into, and potentially pinchedbetween, the overtube and any loose fitting components inserted into itsinner lumen. As illustrated in the embodiments of FIGS. 8 and 8A, thedistal end of the overtube 100 may be used in combination with a Bougie124 attached to the distal tip of instruments, such as a flexibleendoscope 126 for visualization, inserted to the distal end of theovertube. For reference, a Bougie is a smooth bullet-shaped leading tipthat facilitates introduction into a lumen. The Bougie OD should besized such that it creates a snug fit with the ID of the overtube'sdistal end.

Alternatively the overtube may be inserted over a guide wire 128 (FIG.8B); the guidewire inserted under direct visualization using anendoscope. A transition member 130 is positioned between the insidediameter of the overtube and the outside diameter of the guidewireproviding for a smooth transition. This transition member preferablyincludes a long taper, and is composed of a soft, flexible material suchas silicone. As shown in FIG. 8A, a similar transition member may beused in place of the Bougie of FIG. 8.

An alternate means of achieving a gently curved leading edge is by meansof a protective, thin walled umbrella-like cap 132 positioned at thedistal end of the overtube. During insertion, the umbrella is positionedso that it fits snugly over the distal opening of the overtube,maintaining a dome shape and creating the gently curved bullet shapethat facilitates insertion and prevents damage to tissue (FIG. 9A). Whenthe desired insertion depth has been achieved with the overtube, theumbrella may be removed by either pulling it back using an element suchas a wire 134 or cable and thus inverting it so that it fits into theovertube's lumen (FIG. 9B), or by pushing it forward with an elementsuch as a wire 134 or cable from the distal end of the overtube, causingthe umbrella to close before withdrawing it through the overtube (FIG.9C).

Expandable Elements

FIG. 10 illustrates how the distal end of the overtube assembly 100 mayoptionally include attachments or features, such as an array 136 ofspreadable fingers 138. Such an expandable element can be used to pushthe stomach wall away from the overtube, expanding and increasing theamount of space available within the stomach to perform a procedure. Anovertube may incorporate or omit such expanders. The benefits ofincreasing the volume within the stomach include improvements in theability to introduce and manipulate tools, improvements in the abilityto locate plications and staples, improved ability to deploy implantabledevices and improved visualization. Essentially, there is more room towork, and this simplifies many of the tasks. In addition to increasingthe volume within the stomach, the expanders may be used to reshape thestomach in a way that facilitates the performance of the procedure. Forinstance, when the expander is at least partially expanded, the overtubemay be pulled back slightly to pull up on the LES and reshape thestomach from its normal dome-like shape into something more resembling acone. During introduction of the overtube into the esophagus, theexpander is preferably in its fully retracted state, so that it presentsa smooth cone shape that facilitates insertion. Once the desiredlocation has been reached with the distal end of the overtube (e.g.,once past the LES), the expander may be caused to open partially orfully to increase the available working volume and reshape the stomachas desired. Expansion of such elements also serves to help position andsupport the distal end of the overtube relative to the stomach,stabilizing it and helping it maintain position.

FIG. 11 shows one embodiment of the expandable elements, in the form ofspreadable fingers 138. The position of the fingers may be adjusted andmaintained anywhere between a fully closed position (FIG. 11A) and afully expanded position (FIG. 11B). In this embodiment, this motion iscreated by changing the relative position of two control rings 140, 142by means of at least one actuator, for example a Bowden cable. In theillustrated embodiment, movement of ring 140 pivots a hinge 144 coupledto fingers 138. At least part of the more distal control ring 140 may besized slightly smaller than the more proximal control ring 142 so thatit fits or nests at least partially within the proximal control ring142. During introduction of the overtube into the esophagus, the fingersare preferably in their fully retracted state, so that they present asmooth Bougie-like leading edge that facilitates insertion (FIG. 11A).Once in the desired location, the fingers may be expanded partially orfully to increase the available working volume and reshape the stomach(FIG. 11B). The fingers may be left in this position for the duration ofthe procedure, or they may be adjusted at any time as desired by theuser.

An additional embodiment of spreadable fingers is shown in FIG. 12. Thisversion of the expandable element again incorporates two control rings,one distal 140 a and one proximal 140 b. However, this design differs inthat the spreadable fingers do not reach forward (more distal) of thedistal control ring when they are fully retracted. Rather, thesespreadable fingers include a hinge 146 at or near the midpoint so thatthey form a link located between the control rings, in effect forming atube-like, scaffold structure. Like the embodiment described in theprevious paragraph and depicted in FIG. 11, pulling the distal controlring 140 a towards the proximal control ring 140 b causes the fingers tospread and deploy. The rings may be approximated by any number ofactuator types, such as the pullwires/Bowden cables 148 depicted in FIG.12 which can be used to draw the rings 140 a, 140 b together, such as bydrawing the distal ring 140 a towards the proximal ring 142 a. At leastone Bowden cable may be used, however using two or more Bowden cablesallows for balancing the actuation forces more evenly around the controlring. FIG. 12A shows this version of the spreadable fingers in its fullyretracted position, FIG. 12B shows it partially expanded, and FIG. 12Cshows it fully extended. The control rings may optionally incorporatefeatures that mate when the fingers are fully deployed to provide apositive stop when the full range of motion has been achieved.

Another embodiment of a mechanism that may be used to control the degreeof expansion of such spreadable fingers employs a Bowden cable attachedat the distal end to each finger in order to determine its position.When tension is applied to each Bowden cable, either separately orsimultaneously, the corresponding finger moves radially outward,creating a larger working space.

In cases where an array of spreadable fingers are used to create theexpandable element, such as that shown in FIG. 11, these fingers mayalso be used to maintain orientation during a procedure. Because theimage from an endoscope may be rotated and may change unpredictablyduring the course of a procedure, features that aid in determininglocation and orientation are helpful. Using landmarks such as thespreadable fingers, especially when they have been individuallyidentified, e.g., with color codes or other markings, aids indetermining position of instruments and visualization components. Theyare especially useful for determining angular position, or “clocking”.

In addition to facilitating introduction of the overtube and enablingusers to increase the working volume and reshape the stomach during aprocedure, the expandable elements, such as the fingers described aboveand in FIG. 11, may serve as attachment points for a variety ofadditional devices. In one case, they may have pads 150 attached attheir distal ends that increase the surface area they present to thestomach wall when deployed, resulting in a more desirable distributionof forces and a more desirable shape (FIG. 13A). In another case, thepads 150 a may be shaped to form a cone when the expandable elements areretracted to their closed position, facilitating introduction of theovertube into the patient (FIG. 13B). In another case, the pads may beconfigured to form suction cups 150 b, which may be applied to thestomach wall and fixed in place when suction is supplied (FIG. 13C). Theuse of suction immobilizes the stomach tissue relative to the distal endof the overtube. In another case the pads may have a deployable implant152, such as the restrictor discussed above, temporarily mounted that,from this lead position at the distal tip of the overtube, may bedelivered to one or more desired sites (FIG. 13D). Expansion of thefingers may then be used to deploy the implant within the stomach.

One embodiment of a mechanism that may be used to control the degree ofspread of such expandable fingers, or any other embodiment that may beeffectively controlled by means of Bowden cables 148, is shown in FIG.14. This control handle serves to adjust the position of an innercontrol cable relative to an outer compressive housing of a Bowden cable148. To accomplish this, an outer cup 154 is used in conjunction with aslidable plate 156. The slidable plate 156 is threaded, and acts like anut when used in combination with a thumbscrew 158, which moves theslidable plate 156 towards or away from the outer cup 154 when it isturned. The thickness of the slidable plate and the clearance betweenits outer edge and the inside edge of the outer cup serve to keep theslidable plate aligned and prevent it from binding within the cup as itmoves. Binding and misalignment may be further prevented via theaddition of alignment slots 160, mated to pins 162 that protrude fromthe slidable plate. The controller may act on at least one Bowden cable,and the cables may be, but are not necessarily, centered or balancedwith respect to the slidable plate. Adjustment of the Bowden cable maybe accomplished with a barrel adjuster, or similar component. If abarrel adjuster is used, it may be comprised primarily of a screw whichhas a hole drilled through its central axis. The Bowden cable'scompressive housing terminates against the screw head while the innercontrol cables runs through the screw. When the screw is inserted into athreaded hole, and the cable is attached to a component (such as theslidable plate shown in FIG. 14), the relative positions of the innercable and outer compressive housing are adjusted.

When retraction of the expandable elements is desired, it may beadvantageous or required, depending on the construction, to incorporatecomponents within the mechanism of the expanders to ensure that theyreliably retract. For instance, in cases where Bowden cables are used toactuate an expandable element, friction between the control cable andthe compressive housing may prevent the expandable element fromreturning to a retracted position. For the embodiment shown in FIG. 11,this may be accomplished by means of a compression spring that pushesthe two control rings apart. Alternately, nitinol spring elements may beincorporated to act upon the outer face of each of the fingers when theyare extended, so that they push the fingers back to the retractedposition when tension is removed from the Bowden cable that pulls thecontrol rings together.

An alternate embodiment of an expandable element located at the distalend of the overtube or on a separate elongate member passed through theovertube, is shown in FIG. 15. In this embodiment, a fully expanded pairof hoops are comprised of numerous piecewise sections 166 which havecentral tensioning cables 168 running through their centers. When thetensioning cables are relaxed, the hoop sections are free to moverelative to each other, and the result is a flexible chain of shortelements. This configuration is well suited for insertion of the devicethrough the overtube. When the tensioning cable is placed in tension,the hoop sections are forced to join together and organize into a shapethat creates additional volume within the stomach, such as the hoops, orglobe, shape shown. In this example, a hoop shape is depicted, howeverother shapes are possible and may be desirable, such as triangles,squares, umbrellas, etc.

Articulatable Section

At least one articulatable, lockable section may optionally beincorporated within the insertable length of the overtube. FIG. 16 showsa version of the overtube that incorporates such an articulatablelength, labeled 103. The purpose of the articulatable section is tofacilitate positional control of instruments and devices insertedthrough the lumen defined by the overtube. For instance, anarticulatable section may be steered (caused to bend at a desirableangle and direction), to impart a “hockey stick” shape to the insertablelength of the overtube. Additionally, the shape of the articulatablesection may be locked in place by immobilizing or otherwise constrainingthe actuating elements that determine its shape. The simplestembodiments of the overtube may incorporate no such articulatingsection, being comprised entirely of a passive tube, as described aboveand depicted in FIG. 3. However, at least one articulatable section maybe incorporated in such a way that it is coaxial and continuous withother passive, non-articulatable sections of the overtube. Thearticulatable section(s) have an OD, ID and wall thickness similar, butnot necessarily equal, to those of the passive overtube sections. FIG.16 shows the configuration of the articulatable section(s), which may belocated at the distal end of the overtube, such that the section 108 hasminimal length or zero length. Alternately, the articulatable sectionsmay be located between passive sections of the overtube, such that thelength of sections labeled 108 and 102 are non-zero. Similarly, thearticulating section may be located at the proximal end of the overtubeso that the length of the passive section 102 has minimal or zerolength. In cases where more than one articulating section isincorporated, they may be located in any of the positions defined above,and they may be located next to each other or separated by passivesections. The preferred number of articulating sections is either zeroor one, and the preferred location of the articulating section is nearthe distal end of the overtube, such that the length of the passivesection 108 is between 0-6 in.

Steering Controls

Steering control of the articulatable section may be achieved by avariety of methods. The preferred method is to control articulation withat least one pull cable, such as a Bowden cable, acting within a coiltube compression housing. A single such control cable can be used tocontrol the shape of the articulatable section in one direction (e.g.,to the right), or a single cable can be used in combination with anopposing spring element to cause articulation in two directions (e.g.,the spring pulls to the left and the cable pulls to the right).Alternately, two control cables can be used to control articulation intwo directions (e.g., left and right). Extending this further, threecontrol cables can be used in combination to allow for articulation inall directions (e.g., left, right, up and down), or four control cablescan be used, each directly controlling bending of the articulatablesection in each direction. The use of four control cables is thepreferred method, as the resulting control is simple and intuitive forthe user.

The control cables may be used to steer, or determine the curvature of,the articulating section of the overtube. FIG. 22 shows an example wheretwo control cables are used to control the articulation angle Θ of adistal articulatable section in two directions, up (U) and down (D). Thecoil tube housings associated with the control cables are routed from arotating control knob 170 located at the proximal end of the overtubeassembly, down the length of the overtube to the junction between thelength of passive overtube 102 and the articulatable section 103controlled by the knob 170. Rotating the control knob in one directionresults in one control cable being pulled in and an opposing controlcable being spooled out. Similarly, rotating the control knob in theopposite direction reverses these motions. The resulting motion andforces are transmitted down the length of the control cables andcompression housings to the articulatable length of overtube, anddetermine the major (inner) and minor (outer) arc lengths of thearticulating section. As an example, FIG. 22 illustrates the case wherethe control knob is rotated clockwise by the user. This results in theupper control cable 172 being pulled relative to its compression coiltube housing 174, and this defines the minor arc length (l) along thetop edge of the articulating length. Simultaneously, the rotation of theknob 170 releases tension on and feeds out the bottom control cable 176relative to its corresponding compression coil tube housing 178,defining the major arc length (L) along the bottom edge of thearticulating section. Variations of this design may incorporate fourcontrol cables, each determining the bending of the articulatablesection in a different direction, such as left, right, up and down. Forthis case, two knobs are used. One knob controls one pair of controlcables, e.g., the left-right pair, and the other knob controls the otherpair of control cables, e.g., the up-down pair. The steering controlknobs may optionally be oriented so that their position relates to thedirection of steering they control. For example, when two knobs are usedwith one knob controlling left-right bending and the other knobcontrolling the up-down bending, the knobs may be rotated relative toone another by 90°. Further, the knobs may be oriented so that theposition of the knob controlling bending in the left-right directions ishorizontal and the position of the knob controlling bending in theup-down directions is vertical.

The length of each of the Bowden cables is critical to their correctperformance, and for this reason elements that facilitate theiradjustment are helpful. Even in cases where they have been cut to theexact length required and perfectly installed, cables typically stretchover time and use, and will require periodic adjustment. For thisreason, the control knob assemblies may incorporate a number of means ofcable adjustment. One useful characteristic of a control knob is toincorporate a means to deal individually with each control cable thatterminates there. For instance, if the control knob determines the shapeof the articulatable section in the left-right direction, the cablecontrolling bending to the left can be managed and kept separate andadjusted independently of the cable controlling bending to the right.This may be accomplished by incorporating two completely separatesections 170 a, 170 b of the control knob, one for each terminatingcontrol cable, as illustrated in FIG. 23. In this figure, the 2-partspool is indicated with the reference numerals 171 a, 171 b. Coarsecable adjustment can be provided by incorporating a multitude ofattachment points between the knob described in the paragraph above andthe Bowden cable. The spool around which the control cable is woundrequires a single potential attachment point, such as a pin, for acontrol cable, however if multiple potential attachment points areprovided, the length of the cable may be adjusted relative to theposition of the spool and knob. The example shown in FIG. 24A haspotential attachment point 173 spaced every 15°, however this spacingmay be any useful interval. The route of the control cable wire to thecontrol knob termination point is preferably but not necessarily smooth,so that it does not present any hard corners or sharp edges to thecable, extending its operating life. Fine cable adjustment may beaccomplished with the addition of a barrel adjuster or similar element.In the case of a barrel adjuster, a screw is drilled through its centralaxis, and the cable's compressive housing terminates against the screwhead while the inner control cable runs through the screw. When thescrew is inserted into a threaded hole 182, and the cable is attached toa component (such as the spool shown in FIG. 24A), the relativepositions of the inner cable and outer compressive housing may beadjusted by the position of the screw. Turning the screw so that itmoves towards the cable's termination point (e.g., clockwise forright-handed threads) loosens the cable. Conversely, turning the screwso that it moves away from the cable's termination point (e.g.,counter-clockwise for right-handed threads) tightens the cable. This isdepicted in FIG. 24B.

Control of an articulating section may also be achieved by means otherthan Bowden cables. Any appropriate alternate actuation method andenergy source may be used, such as hydraulic or pneumatic actuators,which could be used to create the motion and forces needed to bend thearticulatable section.

Articulatable Section Construction

The articulatable sections may be constructed using a variety oftechniques. One simple embodiment consists of a single coil springelement 112 capable of bending as desired, and is shown in FIG. 17A. Theproximal 184 and distal 186 ends of the spring are fitted with end caps188 that provide termination points for actuating elements (describedbelow) and mounting features for attaching them to other parts of theovertube's insertable length. Additional features may be useful forrouting components that traverse through the articulatable section, suchas Bowden cables running between the user controls at the proximal endand the expandable elements at the distal tip. The spring element 112may have significant space between the coil windings so that it bendsfreely when a moment is applied between the distal and proximal endswithout changing length significantly. To cause the spring toarticulate, a Bowden cable may be used, attached across one side of theoutside of the spring element. If the Bowden cable's compressive housingterminates at the proximal end cap 188 a of the spring element, and thecontrol cable terminates at the distal end cap 188 b of the springelement, pulling on the cable relative to the compressive housingresults in the spring bending in the direction of the cable, as shown inFIG. 17B. A backbone 190 extending through the overtube preventscollapse of the spring during bending. Bending the spring element inother directions is achievable by attaching additional Bowden cables inother locations around the outside of the spring element. A benefit ofthis construction is that the spring element comprising thearticulatable section returns to a straight shape when tension isreleased from the control cables: its relaxed configuration is straight.The spring element comprising the articulatable section of thisconstruction may be created by attaching a separate spring to passivesections of the overtube to create the full insertable length of theovertube, or it may be formed from the same materials used as thesupporting structure of the passive sections of the insertable overtube.This can be accomplished by altering the winding pitch and/or thediameter locally, if needed, where the articulatable section isrequired.

An alternative means of constructing an articulatable section is tocreate it by stringing together on cables 194 a succession of ringsshaped in such a way that they are allowed to rock relative to oneanother. The rocking motion can again be controlled through the use ofBowden cables. This construction technique is illustrated in FIG. 18Athrough D. The shape of each ring is such that it forms an inner lumen,and is preferably (but not necessarily) round. The inner radius r issized so that it is approximately the same as the inner radius of therest of the insertable length of the overtube. The outer radius R andthe wall thickness T are equal to or as close as possible to the outerradius of the rest of the insertable length of the overtube. Four smallthrough holes are drilled through each ring's wall parallel to thecentral axis of the overtube, at the 3, 6, 9 and 12 o'clock positions.These holes accept the control cables 194, which run through each ringand hold the assembly together. When viewed from the side, as shown inFIG. 18A, each ring is flat along the bottom surface and has two alignedraised arches along the top surface. In the figure, these are shown inthe 12 and 6 o'clock orientation. The raised sections are oriented sothat their peaks are coincident with the small holes drilled through thewall. To assemble the articulatable section, a number of rings arestrung together using control cables 194. At the distal end of theassembly of rings, each cable is terminated, e.g., with a crimp 196. Atthe proximal end of the assembly of rings, each compressive housing isterminated. When sufficient tension is applied to a control cable, itwill pull back and move into its compressive housing, and thecorresponding side of the distal end of the assembly of rings is pulledtowards the proximal end. The cables themselves constrain the relativemotion of the rings so that the result is piecewise bending. This isshown in FIG. 18B and FIG. 18D. The rings are prevented from slidingrelative to each other and losing organization by the cables thatconnect them. Such rings may be comprised of any of a variety ofmaterials that possess adequate strength, however stainless steel orpolycarbonate are preferred.

The arrangement of the rings relative to each other in the assemblydetermines whether bending in two directions results (e.g., left andright) or whether bending in four directions (e.g., left, right, up anddown) is allowed. FIGS. 18A and B show the construction that results inarticulation in two directions (left and right). For this construction,the raised portions of each of the rings are all oriented similarly,e.g., from the 12 o'clock position to 6 o'clock position. When controlcables are actuated at the 3 o'clock position or the 9 o'clock position,the assembly is caused to rock in the direction of the cable undertension. For this construction, all of the rings contribute to thebending of the assembly. The other two cables (at 12 o'clock and 6o'clock) are always held at a fixed length and pretension, and applyingfurther tension to them would not result in bending the articulatablesection. Instead, these cables serve primarily to string the ringstogether and stabilize the assembly. They may terminate immediately atthe proximal end of the articulatable section, without the use ofcompressive housings, or they may optionally extend back to the proximalcontrols.

FIGS. 18C and D show a variation of the construction that enables theassembly of rings to articulate in four directions (left, right, up anddown). For this construction, the raised portions of each of the ringsare alternated, rotated 90° between successive rings. When any of thefour control cables is actuated, or combinations of control cables, theassembly is caused to rock in the direction of the cable(s) undertension. For this construction, each ring contributes to the bending ofthe assembly in two of the four possible directions, such as the leftand right pair. Every other ring contributes bending in the left-rightdirections, alternating with rings that contribute bending in theup-down directions. FIG. 18D illustrates the contributions of each ofthe rings in the assembly when a single cable is pulled.

These stacked ring embodiments of the articulatable section may also beused to construct unarticulatable sections. Such sections are flexible,but their articulation is not selectable or controllable by a user. Whenthis approach is used, the entire length of the overtube may beconstructed using a continuous assembly of rings, oriented in at leastone of the ways described above. The shape of at least one region of theassembly may be controllable (e.g., articulatable or steerable) viaBowden cables, as described, while the remaining regions of the assemblywhich are not controllable have no Bowden cables determining theirshape.

Another embodiment of an articulatable section is shown in FIG. 19. Inthis version, rings 198 that are joined with hinge joints 200 arecombined to form an assembly that may be caused to articulate in adesired direction by means of an actuator that pulls differentially in agiven direction, such as a Bowden cable. The orientation of successivehinges may alternate in increments of 90° as shown, which enablesbending in four directions (e.g., left, right, up and down), or allhinges may be aligned in the same orientation, which will allow forbending in two directions (e.g., left and right). As with the previouslydescribed embodiment, the balance of the insertable length of theovertube may also optionally be made using this construction. A singlesection, multiple sections, or no section may then optionally be madearticulatable by means of actuators such as Bowden cables.

Regardless of the construction of the articulatable section, it may haveeither a continuous outer sheath 202 or surface, a continuous innersheath 204 or surface, or both (e.g., sheaths positioned over the innerand outer surfaces of the articulating rings, coil or other articulatingfeatures, or an encapsulation/positioning of such articulating featureswithin the walls of a sheath). This is shown in FIG. 20. The materialused to create the sheath preferably offers little resistance to thebending of the articulatable section. For this reason, soft materials,such as a low durometer, thin wall urethane, silicone or similarmaterial are preferred. The overtube's terminating end piece provides anair tight seal against devices inserted through the inner lumen for thepurpose of facilitating and maintaining insufflation of the stomachduring a procedure, and if the overtube is not a continuously sealedtube along its insertable length, air leaks are likely to occur.Insufflation facilitates visualization and access by increasing thevolume of the stomach where the procedure is performed, and wheninsufflation is not adequate, the procedure may be negatively impacted.

Components may be added to or incorporated within the overtube toprovide tactile feedback to users when instruments within the overtube'sinner lumen are moved. For example, elements may be used that providethe sensation of indexing, such as a ratcheting feel of engagement anddisengagement, when an instrument is inserted into the overtube tospecific depth intervals, or rotated relative to the overtube 100 atangular intervals. One embodiment of such a feature makes use ofmagnetic interactions. If at least one magnet 206 or magneticallyattractive element is incorporated into the overtube, and acorresponding magnet 208 or magnetically attractive element isincorporated into an instrument 210 that moves relative to the overtube,the elements will attract or repel each other as they move into and outof proximity. This is illustrated in FIG. 21. These forces may be usefulto the user to indicate that a location of interest has been achieved,or that a certain increment of motion has occurred. Another embodimentof such a feature involves a ball detent, mounted either in the overtubeor in an insertable instrument that indexes against indentations in amating surface. The indentations may be either circular or elongate inshape.

Depth and Angle Markings

The proximal end of the overtube may incorporate graduated markingsindicating depth and radial angle (FIG. 25). The depth markings 212 aenable users to quantitatively track and control the depth of insertionof the overtube into the patient, as well as the depth of insertion ofinstruments, tools and devices into the overtube. The radial angularmarkings 212 b similarly enable users to quantitatively track andcontrol the angular position (also called “clocking”) of the overtubeand the instruments, tools and devices inserted into the overtube. Thedepth and angle markings also enable users to repeatedly return aninstrument or device to a previously achieved location when required.Additionally, the depth and angle markings enable users to repositioninstruments and devices at a known location relative to a previouslyachieved location. For example, if a physician wishes to create a newstapled mounting point in the stomach wall at a location 90° clockwiseand at an equivalent distance from the LES relative to a previouslyplaced stapled mounting, he or she would ensure that the overtube wasinserted to the same depth and angular position into the patient forboth sequences of operations, that the instruments used were insertedinto the overtube at the same depth, and that the instruments wererotated 90° clockwise as indicated on the overtube's angular markings.

Color Coding to Indicate Orientation

The angular markings at the proximal end of the overtube may be furtheridentified by means of color coding (FIG. 26). For instance, thequadrant from 0° to 90° may be indicated with the color green (G), thequadrant from 90° to 180° with red (R), 180° to 270° with blue (B), and270° to 0° with no color (NC) added. These color codings may becoordinated with similar markings at the distal end of the overtube 110which will be visualized with an endoscope. This improves the ability ofthe user to maintain proper orientation and obtain the desired resultwhen manipulating instruments at the proximal end of the overtube, sinceit directly corresponds to what he or she observes visually at thedistal end of the overtube. The color coding at the distal end of theovertube may be applied anywhere that may be visualized by an endoscopeplaced inserted through the inner lumen, such as to the overtube itself(including passive and/or articulatable sections), or to componentsattached to and extending beyond the distal end of the overtube. Forinstance, expandable elements such as spreadable fingers may be added tothe end of the overtube which may each be a unique color. Alternately,components may be extended from the distal end of the overtube for theexpress purpose of placing color coded markings within the field of viewof the endoscope (FIG. 27). These forward-extending components may be ofany useful shape, e.g., a tubular antenna, or a garden-hoe-like flag.

The steering controls that determine the angle and direction of thearticulatable section may also be marked to correspond to the markingson components at the distal end of the overtube. If, for instance, thespreadable finger located at the top of the overtube (at the 12 o'clockposition) is red, the control knob that determines the up-down positionof the articulatable section will have a red marking on it indicatingwhich direction it should be turned to cause the articulatable sectionto bend in the up direction. Similarly, if the spreadable finger locatedat the bottom of the overtube (at the 6 o'clock position) is blue, thenmarkings on the same knob will incorporate an indication of whichdirection it should be turned to cause the articulatable section to benddown. This may be done, for example, by marking the knobs with differentcolor arrows.

In addition to indicating which direction to turn each knob to achievethe desired bend angle with the articulatable section, each knob may bemarked with an indication of when the articulatable section isapproximately straight. A marking indicating the “neutral” position ofthe articulatable section allows a user to straighten the articulatablesection with high confidence, rather than relying on “feel” or for thearticulatable section to return to a straight configuration if tensionis released on the controlling Bowden cables.

A positive retention force and tactile feedback may also be provided inthe steering control knobs by incorporating ball detent components and asequence of mating indentations. When a user turns a steering controlknob, the ball detents can prevent the knob from turning freely, thuspreventing the articulatable section from unintentionally returning toits relaxed neutral position. The indexing that occurs as the balldetent moves through the succession of indentations may also provideuseful tactile feedback to the user, indicating increments of rotationof a knob and/or certain positions of the articulatable section, such asstraight or neutral.

Terminating End Ring

The proximal end of the overtube incorporates a terminating end ring(FIG. 28). The end ring is attached to, and is not free to move relativeto, the insertable length of the overtube. The end ring incorporates atleast one sealing feature for the purpose of creating and maintaining anair-tight seal against components inserted into its inner lumen. Wheninsufflation or suction is applied through the overtube or byinstruments passing within the overtube, this seal prevents flow betweenthe inside and the outside of a patient. The sealing feature may takethe form of at least one o-ring, but preferably two o-rings.Additionally, the end ring incorporates a port for the introduction ofinsufflation. This port accepts tubing through which insufflation airmay flow. Optionally, a clamp valve may be installed over theinsufflation tubing to control the flow of air, or the flow may becontrolled by means of turning the insufflation pump on and off.

Fixturing Ring

Over the terminating end ring, a fixturing ring 220 (FIG. 29) may befitted that facilitates attachment to a clamping or fixturing device,such as an iron intern. For this reason, this device may also bereferred to as an “iron intern ring”. The iron intern ring fits looselyover the terminating end ring, so that it is possible to rotate themrelative to each other. The fixturing ring also incorporates at leastone tensioning element that, when active, immobilizes the terminatingend ring relative to the fixturing ring. This tensioning element may beembodied, for example, by at least one screw 222 that, when tightened,locks the terminating end ring relative to the iron intern ring,preventing rotation and axial motion. Preferably, more than one screw isused to distribute the clamping load. For example, three clamping screwsare shown in FIG. 29. This screw may also incorporate features thatfacilitate frequent adjustment without requiring the use of tools. Forinstance, large knobs may be located on the screw heads to enable usersto tighten and loosen them by hand. The iron intern ring is also themounting point for elements of the overall device that are inconvenientto rotate in the event that the insertable length of the overtube istorqued. This includes the steering controls for the articulatable,lockable section of the overtube and the position control from theexpandable elements, such as the embodiment shown in FIG. 14. In oneembodiment, the steering controls (e.g., left-right control 226 andup-down control 228) and the expandable element controller 230 areincorporated into a single component, and this component is attached tothe iron intern ring (FIG. 30).

An overtube may be packaged alone or as a system in combination withrelated components such as staplers and implants of the type referencedin the application, as well as any combination of the following:Bougies, transition members, guidewires, endoscopes etc. The systemmight further include instructions for use instructing a user to employthe system in accordance with the methods disclosed herein.

As is apparent from the forgoing disclosure, in some embodimentsdescribed above, the overtube comprises an articulating section, anactuator for effecting articulation of the articulating section, and anoptional locking mechanism allowing the articulating section to belocked in a desired position. In other embodiments described above, theovertube comprises an elongate tube having one or more retractionelements on its distal end, allowing the overtube to create workingspace within the body (e.g., stomach) while giving access to instrumentspassed through its lumen.

It should be recognized that a number of variations of theabove-identified embodiments will be obvious to one of ordinary skill inthe art in view of the foregoing description. Accordingly, the inventionis not to be limited by those specific embodiments and methods of thepresent invention shown and described herein. The applications andmethods listed are not limited to the treatment of diseases orprocedures listed. Modifications of the above described methods andtools and variations of this invention that are obvious to those ofskill in the art are intended to be within the scope of this disclosure.Moreover, the disclosed embodiments may be combined with one another invarying ways to produce additional embodiments.

Any and all patents, patent applications and printed publicationsreferred to above, including those relied upon for purposes of priority,are incorporated herein by reference.

1. An endogastric overtube for use in a stomach of a patient,comprising: a flexible elongate tube having a proximal end and a distalend, the tube proportioned such that when the distal end is in thestomach, the proximal end is positioned outside the patient, the tubeincluding at least one lumen extending from the proximal end to thedistal end, the tube having a maximum outer diameter of at leastapproximately 10 mm; and a control cable extending through a wall of thetube, the control cable coupled to a distal portion of the tube suchthat engagement of the control cable causes deflection of the distalportion.
 2. The endogastric overtube of claim 1, wherein the tubefurther includes a reinforcement on a distal portion of the tube.
 3. Theendogastric overtube of claim 2, wherein the tube is a formed ofpolymeric material and wherein the reinforcement is embedded within thepolymeric material.
 4. The endogastric overtube of claim 2, wherein thetube is a formed of polymeric material and wherein the reinforcement ispositioned on an inner surface of the lumen or an outer surface of thetube.
 5. The endogastric overtube of claim 2, wherein the reinforcementis a resilient coil.
 6. The endogastric overtube of claim 2, wherein thereinforcement is at least one resilient ring.
 7. The endogastricovertube of claim 2, wherein the reinforcement is at least one partialring.
 8. The endogastric overtube of claim 6, wherein the resilient ringis circular.
 9. The endogastric overtube of claim 6, wherein theresilient ring is elliptical.
 10. The endogastric overtube of claim 2,wherein the reinforcement includes a mesh element.
 11. The endogastricovertube of claim 2, wherein the lumen has a diameter, and wherein thetube is expandable from a first position to a second position inresponse to introduction of an instrument having a diameter exceedingthe lumen diameter into the lumen, and wherein the reinforcement isconfigured to restore the tube to the first position upon removal of theinstrument from the lumen.
 12. The endogastric tube of claim 1, furtherincluding a removable atraumatic tip on the distal end.
 13. Theendogastric tube of claim 12, wherein the atraumatic tip is positionedon an elongate member extending through the lumen.
 14. The endogastrictube of claim 12, wherein the atraumatic tip is a cap at least partiallycovering the distal end of the tip.
 15. The endogastric tube of claim12, wherein the elongate element is retractable in a proximal directionto invert the cap into the lumen.
 16. The endogastric tube of claim 12,wherein the elongate element is advanceable in a distal direction tocollapse the cap into a collapsed position, and wherein the elongateelement is retractactable to withdraw the cap in the collapsed positionthrough the lumen.
 17. The endogastric tube of claim 5, wherein thecontrol cable is coupled to the spring element.
 18. The endogastric tubeof claim 1, further including a retractor element on the distal end ofthe tube, the retractor element moveable from a first position to asecond position in which the retractor element extends laterally fromthe tube.
 19. The endogastric tube of claim 18, wherein the retractorelement extends longitudinally when in the first position.
 20. Theendogastric tube of claim 18, wherein the retractor element includes afirst portion coupled to a first ring and a second portion coupled to asecond ring, and wherein relative movement of the second ring towardsthe first ring moves the retractor element from the first position tothe second position.
 21. The endogastric tube of claim 20, wherein theretractor element includes a hinge, and wherein the first portion andthe second portion are on opposite sides of the hinge.
 22. Theendogastric tube of claim 20, wherein the first portion is an elongatemember, and wherein the second portion is a pivot element pivotablycoupled between the elongate member and the second ring.
 23. Theendogastric tube of claim 18 wherein the retractor element includes amount for receiving an implant to be implanted in the stomach.
 24. Theendogastric tube of claim 1, further including a retractor element onthe distal end of the tube, the retractor element including a pluralityof segments and a cable extending between the segments, the retractorhaving a first, flexible, position and a second, more rigid, position,the cable retractable to move the retractor from the first to the secondposition.
 25. The endogastric tube of claim 24, wherein the segments arepositioned on a cable loop and wherein the retractor element in thesecond position forms a retractor hoop.
 26. The endogastric tube ofclaim 25, further including a second retractor element including aplurality of second segments and a second cable extending between thesegments, the second cable retractable to move the second retractor froma flexible position to a more rigid position.
 27. The endogastric tubeof claim 26, wherein the second retractor in the second position forms aretractor hoop.
 28. The endogastric tube of claim 1, wherein the tubeincludes a seal positioned to seal against an instrument inserted intothe lumen.
 29. The endogastric tube of claim 1, wherein the proximalportion of the tube includes a port positionable in fluid communicationwith a source of insufflation gas.
 30. The endogastric tube of claim 1,wherein the tube has a maximum outer diameter of between approximately10 mm-20 mm.
 31. The endogastric tube of claim 30, wherein the tube hasa maximum out diameter of between approximately 15 mm-20 mm.
 32. Theendogastric tube of claim 30, wherein the tube has a maximum outerdiameter of approximately 20 mm.
 33. The endogastric tube of claim 1,wherein the tube has a maximum outer diameter of approximately 18-22 mm.34. The endogastric tube of claim 1, wherein the tube has a maximum wallthickness of 0.1-0.2 mm.
 35. An endogastric overtube for use in astomach of a patient, comprising: a flexible elongate tube having aproximal end and a distal end, the tube proportioned such that when thedistal end is in the stomach, the proximal end is positioned outside thepatient, the tube including at least one lumen extending from theproximal end to the distal end, the tube having a maximum outer diameterof at least approximately 10 mm; and a retractor element on the distalend of the tube, the retractor element moveable from a first position toa second position in which the retractor element extends laterally fromthe tube.
 36. The endogastric tube of claim 35, wherein the retractorelement extends longitudinally when in the first position.
 37. Theendogastric tube of claim 35, wherein the retractor element includes afirst portion coupled to a first ring and a second portion coupled to asecond ring, and wherein relative movement of the second ring towardsthe first ring moves the retractor element from the first position tothe second position.
 38. The endogastric tube of claim 37, wherein theretractor element includes a hinge, and wherein the first portion andthe second portion are on opposite sides of the hinge.
 39. Theendogastric tube of claim 37, wherein the first portion is an elongatemember, and wherein the second portion is a pivot element pivotablycoupled between the elongate member and the second ring.
 40. Theendogastric tube of claim 37, wherein the retractor element includes amount for receiving an implant to be implanted in the stomach.
 41. Theendogastric tube of claim 35, further including a retractor element onthe distal end of the tube, the retractor element including a pluralityof segments and a cable extending between the segments, the retractorhaving a first, flexible, position and a second, more rigid, position,the cable retractable to move the retractor from the first to the secondposition.
 42. The endogastric tube of claim 41, wherein the segments arepositioned on a cable loop and wherein the retractor element in thesecond position forms a retractor hoop.
 43. The endogastric tube ofclaim 42, further including a second retractor element including aplurality of second segments and a second cable extending between thesegments, the second cable retractable to move the second retractor froma flexible position to a more rigid position.
 44. The endogastric tubeof claim 43, wherein the second retractor in the second position forms aretractor hoop.
 45. The endogastric tube of claim 35, wherein the tubeincludes a seal positioned to seal against an instrument inserted intothe lumen.
 46. The endogastric tube of claim 35, wherein the proximalportion of the tube includes a port positionable in fluid communicationwith a source of insufflation gas.
 47. The endogastric tube of claim 35,wherein the tube has a maximum outer diameter of between approximately10 mm-20 mm.
 48. The endogastric tube of claim 47, wherein the tube hasa maximum out diameter of between approximately 15 mm-20 mm.
 49. Theendogastric tube of claim 35, wherein the tube has a maximum outerdiameter of approximately 20 mm.
 50. The endogastric tube of claim 35,wherein the tube has a maximum outer diameter of approximately 18-22 mm.51. The endogastric tube of claim 35, wherein the tube has a maximumwall thickness of 0.1-0.2 mm.